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National Center of Genetics

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The National Center of Genetics (NCG) of the LNS covers all areas of human genetics, including clinical genetics, genetic counselling and an extensive spectrum of genetic diagnostics, from conventional karyotyping to modern next generation sequencing (NGS).

The NCG offers genetic consultations and diagnostics to individuals and their families, e.g. in the context of familial predisposition to cancer, rare hereditary diseases, or prenatal genetics and family planning. In addition, we are continuously establishing new techniques and expanding our diagnostic portfolio to ensure state-of-the-art patient care.

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MEET OUR team

MEET OUR team

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Dr. Abdelkader Heddar,
MD, PhD

Geneticist

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Marizela Kulisic, PhD

Clinical Laboratory Scientist

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Thierry Streng

Laboratory Assistant

What makes NIPT unique is its ability to screen for chromosomal anomalies with high sensitivity and specificity, using nothing more than a maternal blood sample. For us, it means bringing cutting-edge genomics into routine prenatal care — safely, early, and without risk for the pregnancy.

KEY FIGURES

2,540

Genetic Consultations

38,642

Genetic Tests

8,260

Non-invasive Prenatal Tests